Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_assertion description "[The highest risk of meningioma was associated with heterozygosity for both MTHFR variants odds ratio (OR), 2.11; 95% confidence interval (95% CI), 1.42-3.12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_assertion evidence source_evidence_literature NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_assertion SIO_000772 18483342 NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_assertion wasDerivedFrom gad-20150221 NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_assertion wasGeneratedBy ECO_0000203 NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP91483.RArUJa-NlFMC_U2RMK6pGVk6xXrrs3B4rny3RXUDrmZLY130_provenance.